On the public citation graph

Aphids: A Model for Polyphenism and Epigenetics

https://doi.org/10.1155/2012/431531

0 signed · 234 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/bdrc.20026openalex-snapshot

Mechanisms for the environmental regulation of gene expression

inferredcites →https://doi.org/10.1002/bies.200900189openalex-snapshot

Rediscovering Waddington in the post‐genomic age

inferredcites →https://doi.org/10.1002/jcp.21678openalex-snapshot

Epigenetic control

inferredcites →https://doi.org/10.1002/jez.b.3openalex-snapshot

A comparison of parthenogenetic and sexual embryogenesis of the pea aphid Acyrthosiphon pisum (Hemiptera: Aphidoidea)

inferredcites →https://doi.org/10.1002/jmor.1051860206openalex-snapshot

Morphology, ultrastructure, and germ cell cluster formation in ovarioles of aphids

inferredcites →https://doi.org/10.1002/pmic.200800692openalex-snapshot

The secreted salivary proteome of the pea aphid Acyrthosiphon pisum characterised by mass spectrometry

inferredcites →https://doi.org/10.1007/978-3-540-75157-1_4openalex-snapshot

Role of Dicer in Posttranscriptional RNA Silencing

inferredcites →https://doi.org/10.1007/978-3-540-75157-1_8openalex-snapshot

RNAi-Mediated Chromatin Silencing in Fission Yeast

inferredcites →https://doi.org/10.1007/bf02510847openalex-snapshot

Maternal age as a source of variation in the ability of an aphid to produce dispersing forms

inferredcites →https://doi.org/10.1007/bf02754093openalex-snapshot

Maternal age as a source of variation in the ability of an aphid to produce dispersing forms

inferredcites →https://doi.org/10.1007/s00018-010-0505-5openalex-snapshot

Stable transmission of reversible modifications: maintenance of epigenetic information through the cell cycle

inferredcites →https://doi.org/10.1007/s00442-003-1185-8openalex-snapshot

The interplay between density- and trait-mediated effects in predator-prey interactions: a case study in aphid wing polymorphism

inferredcites →https://doi.org/10.1007/s00442-004-1710-4openalex-snapshot

Predator-induced transgenerational phenotypic plasticity in the cotton aphid

inferredcites →https://doi.org/10.1007/s10577-007-1176-4openalex-snapshot

Analysis of heterochromatic epigenetic markers in the holocentric chromosomes of the aphid Acyrthosiphon pisum

inferredcites →https://doi.org/10.1016/0022-1910(59)90024-1openalex-snapshot

The role of photoperiod and temperature in the determination of parthenogenetic and sexual forms in the aphid Megoura viciae Buckton—I

inferredcites →https://doi.org/10.1016/0022-1910(63)90067-2openalex-snapshot

The role of photoperiod and temperature in the determination of parthenogenetic and sexual forms in the aphid Megoura viciae Buckton—III. Further properties of the maternal switching mechanism in apterous aphids

inferredcites →https://doi.org/10.1016/0022-1910(67)90155-2openalex-snapshot

The production of the apterous and alate forms in the aphid Megoura viciae Buckton, with special reference to the rôle of crowding

inferredcites →https://doi.org/10.1016/0022-1910(69)90199-1openalex-snapshot

The role of crowding in the production of winged forms by two strains of the pea aphid, Acyrthosiphon pisum

inferredcites →https://doi.org/10.1016/0022-1910(70)90134-4openalex-snapshot

An intrinsic factor influencing alate production by two strains of the pea aphid, Acyrthosiphon pisum

inferredcites →https://doi.org/10.1016/0022-1910(76)90065-2openalex-snapshot

Wing development and parthenogenesis induced in progenies of kinoprene-treated gynoparae of Aphis fabae and Myzus persicae

inferredcites →https://doi.org/10.1016/0022-1910(79)90046-5openalex-snapshot

Inhibition by kinoprene of photoperiod-induced male production by apterous and alate viviparae of the aphid Myzus persicae

inferredcites →https://doi.org/10.1016/0160-9327(77)90005-9openalex-snapshot

W. H. Fox Talbot and the history of photography

inferredcites →https://doi.org/10.1016/0965-1748(95)00059-3openalex-snapshot

Changes in the methylation of amplified esterase DNA during loss and reselection of insecticide resistance in peach-potato aphids, Myzus persicae

inferredcites →https://doi.org/10.1016/j.bbagrm.2010.05.005openalex-snapshot

Interplay between microRNAs and the epigenetic machinery: An intricate network

inferredcites →https://doi.org/10.1016/j.biocel.2010.03.005openalex-snapshot

Small RNAs in the animal gonad: Guarding genomes and guiding development

inferredcites →https://doi.org/10.1016/j.cell.2006.09.033openalex-snapshot

Analysis of the C. elegans Argonaute Family Reveals that Distinct Argonautes Act Sequentially during RNAi

inferredcites →https://doi.org/10.1016/j.cell.2007.02.005openalex-snapshot

Chromatin Modifications and Their Function

inferredcites →https://doi.org/10.1016/j.cell.2007.05.056openalex-snapshot

Drosophila microRNAs Are Sorted into Functionally Distinct Argonaute Complexes after Production by Dicer-1

inferredcites →https://doi.org/10.1016/j.cell.2007.05.057openalex-snapshot

Sorting of Drosophila Small Silencing RNAs

inferredcites →https://doi.org/10.1016/j.cell.2008.03.029openalex-snapshot

Highly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis

inferredcites →https://doi.org/10.1016/j.cell.2009.01.045openalex-snapshot

Small RNAs as Guardians of the Genome

inferredcites →https://doi.org/10.1016/j.cell.2010.09.009openalex-snapshot

Systematic Protein Location Mapping Reveals Five Principal Chromatin Types in Drosophila Cells

inferredcites →https://doi.org/10.1016/j.cub.2004.12.057openalex-snapshot

MicroRNA Biogenesis: Drosha Can't Cut It without a Partner

inferredcites →https://doi.org/10.1016/j.devcel.2010.10.011openalex-snapshot

Small RNA-Mediated Quiescence of Transposable Elements in Animals

inferredcites →https://doi.org/10.1016/j.devcel.2010.10.014openalex-snapshot

Histone Variants in Metazoan Development

inferredcites →https://doi.org/10.1016/j.gene.2007.10.030openalex-snapshot

Sex versus parthenogenesis: A transcriptomic approach of photoperiod response in the model aphid Acyrthosiphon pisum (Hemiptera: Aphididae)

inferredcites →https://doi.org/10.1016/j.ibmb.2004.05.001openalex-snapshot

Annotated expressed sequence tags for studies of the regulation of reproductive modes in aphids

inferredcites →https://doi.org/10.1016/j.ibmb.2008.08.008openalex-snapshot

A water-specific aquaporin involved in aphid osmoregulation

inferredcites →https://doi.org/10.1016/j.ibmb.2009.09.007openalex-snapshot

Ingested double-stranded RNAs can act as species-specific insecticides

inferredcites →https://doi.org/10.1016/j.molcel.2008.10.018openalex-snapshot

Comparative Analysis of Argonaute-Dependent Small RNA Pathways in Drosophila

inferredcites →https://doi.org/10.1016/j.mrrev.2008.02.004openalex-snapshot

Epigenetic interplay between histone modifications and DNA methylation in gene silencing

inferredcites →https://doi.org/10.1016/j.tig.2011.01.003openalex-snapshot

Insects as innovative models for functional studies of DNA methylation

inferredcites →https://doi.org/10.1016/s0022-1910(01)00055-5openalex-snapshot

Aphid photoperiodic clocks

inferredcites →https://doi.org/10.1016/s0022-1910(99)00161-4openalex-snapshot

The effect of temperature on the photoperiodic ‘clock’ and ‘counter’ of a Scottish clone of the vetch aphid, Megoura viciae

inferredcites →https://doi.org/10.1016/s0140-6736(09)60234-8openalex-snapshot

Towards a new developmental synthesis: adaptive developmental plasticity and human disease

inferredcites →https://doi.org/10.1016/s0960-9822(01)00299-8openalex-snapshot

Double-stranded RNA-mediated silencing of genomic tandem repeats and transposable elements in the D. melanogaster germline

inferredcites →https://doi.org/10.1016/s0965-1748(02)00243-6openalex-snapshot

Identification of a gene overexpressed in aphids reared under short photoperiod

inferredcites →https://doi.org/10.1038/35046205openalex-snapshot

DNA methylation in Drosophila melanogaster

inferredcites →https://doi.org/10.1038/emboj.2009.365openalex-snapshot

Functional involvement of Tudor and dPRMT5 in the piRNA processing pathway in Drosophila germlines

inferredcites →https://doi.org/10.1038/emboj.2011.135openalex-snapshot

Chromatin: constructing the big picture

inferredcites →https://doi.org/10.1038/hdy.2010.2openalex-snapshot

Environmental epigenetics

inferredcites →https://doi.org/10.1038/nature06745openalex-snapshot

Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning

inferredcites →https://doi.org/10.1038/nature07007openalex-snapshot

An endogenous small interfering RNA pathway in Drosophila

inferredcites →https://doi.org/10.1038/nature08514openalex-snapshot

Human DNA methylomes at base resolution show widespread epigenomic differences

inferredcites →https://doi.org/10.1038/nature08911openalex-snapshot

Chromatin remodelling during development

inferredcites →https://doi.org/10.1038/nbt.1626openalex-snapshot

Single base–resolution methylome of the silkworm reveals a sparse epigenomic map

inferredcites →https://doi.org/10.1038/ncb1872openalex-snapshot

Arginine methylation of Piwi proteins catalysed by dPRMT5 is required for Ago3 and Aub stability

inferredcites →https://doi.org/10.1038/ng.743openalex-snapshot

Drosophila Piwi functions in Hsp90-mediated suppression of phenotypic variation

inferredcites →https://doi.org/10.1038/ng1110-920openalex-snapshot

Lack of evidence for DNA methylation of Invader4 retroelements in Drosophila and implications for Dnmt2-mediated epigenetic regulation

inferredcites →https://doi.org/10.1038/nrg2504openalex-snapshot

Small silencing RNAs: an expanding universe

inferredcites →https://doi.org/10.1038/nrg2651openalex-snapshot

Rethinking how DNA methylation patterns are maintained

inferredcites →https://doi.org/10.1038/nrg2719openalex-snapshot

Establishing, maintaining and modifying DNA methylation patterns in plants and animals

inferredcites →https://doi.org/10.1038/nrg2752openalex-snapshot

Chromatin structure and the inheritance of epigenetic information

inferredcites →https://doi.org/10.1038/nrg2904openalex-snapshot

Non-coding RNAs as regulators of embryogenesis

inferredcites →https://doi.org/10.1038/nrg2905openalex-snapshot

Charting histone modifications and the functional organization of mammalian genomes

inferredcites →https://doi.org/10.1038/nrm2321openalex-snapshot

Argonaute proteins: key players in RNA silencing

inferredcites →https://doi.org/10.1038/nrm2640openalex-snapshot

Epigenetic inheritance during the cell cycle

inferredcites →https://doi.org/10.1038/nrm2868openalex-snapshot

MicroRNA control of signal transduction

inferredcites →https://doi.org/10.1038/sj.hdy.6800863openalex-snapshot

Wing dimorphism in aphids

inferredcites →https://doi.org/10.1038/sj.onc.1208053openalex-snapshot

ICBP90, an E2F-1 target, recruits HDAC1 and binds to methyl-CpG through its SRA domain

inferredcites →https://doi.org/10.1042/bc20070135openalex-snapshot

Shifting from clonal to sexual reproduction in aphids: physiological and developmental aspects

inferredcites →https://doi.org/10.1042/bj3390737openalex-snapshot

Relationship between amount of esterase and gene copy number in insecticide-resistant Myzus persicae (Sulzer)

inferredcites →https://doi.org/10.1042/bj3490863openalex-snapshot

Methylation and expression of amplified esterase genes in the aphid Myzus persicae (Sulzer)

inferredcites →https://doi.org/10.1046/j.1365-2311.1998.00113.xopenalex-snapshot

Life cycle of the cereal aphid Sitobion avenae F.: polymorphism and comparison of life history traits associated with sexuality

inferredcites →https://doi.org/10.1046/j.1365-2311.2001.00321.xopenalex-snapshot

The role of nutrition, crowding and interspecific interactions in the development of winged aphids

inferredcites →https://doi.org/10.1046/j.1525-142x.2003.03003.xopenalex-snapshot

Development and evolution of adaptive polyphenisms

inferredcites →https://doi.org/10.1073/pnas.0409034102openalex-snapshot

Transcriptome analysis of the aphid bacteriocyte, the symbiotic host cell that harbors an endocellular mutualistic bacterium, Buchnera

inferredcites →https://doi.org/10.1073/pnas.0605506103openalex-snapshot

MIWI associates with translational machinery and PIWI-interacting RNAs (piRNAs) in regulating spermatogenesis

inferredcites →https://doi.org/10.1073/pnas.0708958105openalex-snapshot

A protein from the salivary glands of the pea aphid, Acyrthosiphon pisum , is essential in feeding on a host plant

inferredcites →https://doi.org/10.1073/pnas.0900301106openalex-snapshot

DNA methylation is widespread and associated with differential gene expression in castes of the honeybee, Apis mellifera

inferredcites →https://doi.org/10.1073/pnas.1002720107openalex-snapshot

Conservation and divergence of methylation patterning in plants and animals

inferredcites →https://doi.org/10.1086/280044openalex-snapshot

The Factors of Inheritance and Parentage as Affecting the Ratio of Alate to Apterous Individuals in Aphids

inferredcites →https://doi.org/10.1086/383618openalex-snapshot

Dynamics of Production of Sexual Forms in Aphids: Theoretical and Experimental Evidence for Adaptive “Coin‐Flipping” Plasticity

inferredcites →https://doi.org/10.1093/gbe/evq057openalex-snapshot

Functional Conservation of DNA Methylation in the Pea Aphid and the Honeybee

inferredcites →https://doi.org/10.1093/jis/3.1.23openalex-snapshot

Aphid biology: Expressed genes from alate Toxoptera citricida, the brown citrus aphid

inferredcites →https://doi.org/10.1093/molbev/msp256openalex-snapshot

Expansion of the miRNA Pathway in the Hemipteran Insect Acyrthosiphon pisum

inferredcites →https://doi.org/10.1093/molbev/msr140openalex-snapshot

Genome Expansion and Differential Expression of Amino Acid Transporters at the Aphid/Buchnera Symbiotic Interface

inferredcites →https://doi.org/10.1093/nar/gkm576openalex-snapshot

Repeat-associated siRNAs cause chromatin silencing of retrotransposons in the Drosophila melanogaster germline

inferredcites →https://doi.org/10.1093/nar/gkq1061openalex-snapshot

The Gypsy Database (GyDB) of mobile genetic elements: release 2.0

inferredcites →https://doi.org/10.1093/oso/9780195122343.001.0001openalex-snapshot

Developmental Plasticity and Evolution

inferredcites →https://doi.org/10.1098/rspb.1997.0103openalex-snapshot

Genotypic variation among different phenotypes within aphid clones

inferredcites →https://doi.org/10.1098/rspb.1999.0814openalex-snapshot

Ladybird-induced life–history changes in aphids

inferredcites →https://doi.org/10.1098/rstb.2009.0241openalex-snapshot

Genotype–phenotype mapping and the end of the ‘genes as blueprint’ metaphor

inferredcites →https://doi.org/10.1098/rstb.2009.0255openalex-snapshot

Aphid wing dimorphisms: linking environmental and genetic control of trait variation

inferredcites →https://doi.org/10.1101/gad.1158803openalex-snapshot

Exportin-5 mediates the nuclear export of pre-microRNAs and short hairpin RNAs

inferredcites →https://doi.org/10.1101/gad.1210204openalex-snapshot

Distinct roles for Argonaute proteins in small RNA-directed RNA cleavage pathways

inferredcites →https://doi.org/10.1101/gad.1334005openalex-snapshot

Dicer-1 and R3D1-L catalyze microRNA maturation in Drosophila

inferredcites →https://doi.org/10.1101/gad.1564307openalex-snapshot

Drosophila PIWI associates with chromatin and interacts directly with HP1a

inferredcites →https://doi.org/10.1101/gad.1956010openalex-snapshot

Structural basis for methylarginine-dependent recognition of Aubergine by Tudor

inferredcites →https://doi.org/10.1101/gad.947102openalex-snapshot

DNA methylation patterns and epigenetic memory

inferredcites →https://doi.org/10.1101/gad.990802openalex-snapshot

RNAi is activated during Drosophila oocyte maturation in a manner dependent on aubergine and spindle-E

inferredcites →https://doi.org/10.1101/gr.6163007openalex-snapshot

CpG methylation is targeted to transcription units in an invertebrate genome

inferredcites →https://doi.org/10.1111/j.0962-1075.2004.00470.xopenalex-snapshot

DNA methylation in insects

inferredcites →https://doi.org/10.1111/j.1365-2583.1996.tb00054.xopenalex-snapshot

Polymerase chain reaction‐based identification of insecticide resistance genes and DNA methylation in the aphid Myzus persicae (Sulzer)

inferredcites →https://doi.org/10.1111/j.1365-2583.2008.00835.xopenalex-snapshot

Wounding‐mediated gene expression and accelerated viviparous reproduction of the pea aphid Acyrthosiphon pisum

inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00935.xopenalex-snapshot

Wing development genes of the pea aphid and differential gene expression between winged and unwinged morphs

inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00946.xopenalex-snapshot

A full‐length cDNA resource for the pea aphid, Acyrthosiphon pisum

inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00972.xopenalex-snapshot

Chromatin‐remodelling proteins of the pea aphid, Acyrthosiphon pisum (Harris)

inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00974.xopenalex-snapshot

A functional DNA methylation system in the pea aphid, Acyrthosiphon pisum

inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00976.xopenalex-snapshot

Comparative analysis of the Acyrthosiphon pisum genome and expressed sequence tag‐based gene sets from other aphid species

inferredcites →https://doi.org/10.1111/j.1461-0248.2005.00754.xopenalex-snapshot

Alarm pheromone mediates production of winged dispersal morphs in aphids

inferredcites →https://doi.org/10.1111/j.1525-142x.2007.00170.xopenalex-snapshot

Common genome‐wide patterns of transcript accumulation underlying the wing polyphenism and polymorphism in the pea aphid (Acyrthosiphon pisum)

inferredcites →https://doi.org/10.1111/j.1525-142x.2009.00375.xopenalex-snapshot

Differential regulations of wing and ovarian development and heterochronic changes of embryogenesis between morphs in wing polyphenism of the vetch aphid

inferredcites →https://doi.org/10.1126/science.1090599openalex-snapshot

Nuclear Export of MicroRNA Precursors

inferredcites →https://doi.org/10.1126/science.1092653openalex-snapshot

Heterochromatic Silencing and HP1 Localization in Drosophila Are Dependent on the RNAi Machinery

inferredcites →https://doi.org/10.1126/science.1120976openalex-snapshot

Methylation of tRNA Asp by the DNA Methyltransferase Homolog Dnmt2

inferredcites →https://doi.org/10.1126/science.1129333openalex-snapshot

A Distinct Small RNA Pathway Silences Selfish Genetic Elements in the Germline

inferredcites →https://doi.org/10.1126/science.1135213openalex-snapshot

Functional CpG Methylation System in a Social Insect

inferredcites →https://doi.org/10.1126/science.1153069openalex-snapshot

Nutritional Control of Reproductive Status in Honeybees via DNA Methylation

inferredcites →https://doi.org/10.1126/science.1165171openalex-snapshot

An Epigenetic Role for Maternally Inherited piRNAs in Transposon Silencing

inferredcites →https://doi.org/10.1126/science.1186366openalex-snapshot

Genome-Wide Evolutionary Analysis of Eukaryotic DNA Methylation

inferredcites →https://doi.org/10.1126/science.1197761openalex-snapshot

The Ecoresponsive Genome of Daphnia pulex

inferredcites →https://doi.org/10.1126/science.1203919openalex-snapshot

Role for piRNAs and Noncoding RNA in de Novo DNA Methylation of the Imprinted Mouse Rasgrf1 Locus

inferredcites →https://doi.org/10.1126/science.286.5439.481openalex-snapshot

Epigenetics: Regulation Through Repression

inferredcites →https://doi.org/10.1146/annurev.biochem.74.010904.153721openalex-snapshot

EUKARYOTIC CYTOSINE METHYLTRANSFERASES

inferredcites →https://doi.org/10.1159/000323510openalex-snapshot

Composition and Epigenetic Markers of Heterochromatin in the Aphid Aphis nerii (Hemiptera: Aphididae)

inferredcites →https://doi.org/10.1186/1471-213x-3-7openalex-snapshot

Diapause in the pea aphid (Acyrthosiphon pisum) is a slowing but not a cessation of development

inferredcites →https://doi.org/10.1186/1471-2148-6-18openalex-snapshot

The evolution of the histone methyltransferase gene Su(var)3-9 in metazoans includes a fusion with and a re-fission from a functionally unrelated gene

inferredcites →https://doi.org/10.1186/1471-2164-10-456openalex-snapshot

Transcriptomic and proteomic analyses of seasonal photoperiodism in the pea aphid

inferredcites →https://doi.org/10.1186/1471-2164-10-472openalex-snapshot

Epigenetic regulation of the honey bee transcriptome: unravelling the nature of methylated genes

inferredcites →https://doi.org/10.1186/1471-2164-11-281openalex-snapshot

Bioinformatic prediction, deep sequencing of microRNAs and expression analysis during phenotypic plasticity in the pea aphid, Acyrthosiphon pisum

inferredcites →https://doi.org/10.1186/1471-2164-8-423openalex-snapshot

Genomic resources for Myzus persicae: EST sequencing, SNP identification, and microarray design

inferredcites →https://doi.org/10.1186/1472-6750-7-63openalex-snapshot

Gene knockdown by RNAi in the pea aphid Acyrthosiphon pisum

inferredcites →https://doi.org/10.1186/gb-2006-7-3-r21openalex-snapshot

Large-scale gene discovery in the pea aphid Acyrthosiphon pisum(Hemiptera)

inferredcites →https://doi.org/10.1186/gb-2007-8-6-r97openalex-snapshot

Computational and transcriptional evidence for microRNAs in the honey bee genome

inferredcites →https://doi.org/10.1186/gb-2008-9-2-210openalex-snapshot

The Argonaute protein family

inferredcites →https://doi.org/10.1186/gb-2009-10-1-r6openalex-snapshot

Characterization and comparative profiling of the small RNA transcriptomes in two phases of locust

inferredcites →https://doi.org/10.1242/dev.005629openalex-snapshot

The growing catalog of small RNAs and their association with distinct Argonaute/Piwi family members

inferredcites →https://doi.org/10.1242/dev.006486openalex-snapshot

Biogenesis and germline functions of piRNAs

inferredcites →https://doi.org/10.1242/jeb.41.1.119openalex-snapshot

The Location of the Photoperiodic Receptors in the Aphid Megoura Viciae Buckton

inferredcites →https://doi.org/10.1242/jeb.67.1.117openalex-snapshot

The Role of Neurosecretion in the Photoperiodic Control of Polymorphism in the Aphid Megoura Viciae

inferredcites →https://doi.org/10.1261/rna.1869710openalex-snapshot

Arginine methylation of Aubergine mediates Tudor binding and germ plasm localization

inferredcites →https://doi.org/10.1261/rna.5167604openalex-snapshot

Exportin 5 is a RanGTP-dependent dsRNA-binding protein that mediates nuclear export of pre-miRNAs

inferredcites →https://doi.org/10.1371/journal.pbio.0030235openalex-snapshot

Processing of Pre-microRNAs by the Dicer-1–Loquacious Complex in Drosophila Cells

inferredcites →https://doi.org/10.1371/journal.pbio.0030236openalex-snapshot

Normal microRNA Maturation and Germ-Line Stem Cell Maintenance Requires Loquacious, a Double-Stranded RNA-Binding Domain Protein

inferredcites →https://doi.org/10.1371/journal.pbio.1000313openalex-snapshot

Genome Sequence of the Pea Aphid Acyrthosiphon pisum

inferredcites →https://doi.org/10.1371/journal.pbio.1000506openalex-snapshot

The Honey Bee Epigenomes: Differential Methylation of Brain DNA in Queens and Workers

inferredcites →https://doi.org/10.1371/journal.pone.0028051openalex-snapshot

Expansion of Genes Encoding piRNA-Associated Argonaute Proteins in the Pea Aphid: Diversification of Expression Profiles in Different Plastic Morphs

inferredcites →https://doi.org/10.1673/031.006.3801openalex-snapshot

RNAi Knockdown of a Salivary Transcript Leading to Lethality in the Pea Aphid, Acyrthosiphon pisum

inferredcites →https://doi.org/10.1673/031.008.3001openalex-snapshot

Cloning and Phylogenetic Analysis of Sid-1-Like Genes from Aphids

inferredcites →https://doi.org/10.1673/2006_06_39.1openalex-snapshot

TrappingPhyllophagaspp. (Coleoptera: Scarabaeidae: Melolonthinae) in the United States and Canada using sex attractants

inferredcites →https://doi.org/10.4161/epi.3.4.6697openalex-snapshot

Epigenetic integration of environmental and genomic signals in honey bees: the critical interplay of nutritional, brain and reproductive networks

inferredcites →https://doi.org/10.4161/mge.1.2.17635openalex-snapshot

GyDB Mobilomics

inferredcites →https://doi.org/10.5694/j.1326-5377.1958.tb86500.xopenalex-snapshot

The Strategy of the Genes: A Discussion of Some Aspects of Theoretical Biology

inferredcites →https://doi.org/10.5860/choice.39-5182openalex-snapshot

From DNA to diversity: molecular genetics and the evolution of animal design

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/biorisk.24.171467zenodo-depositor-declared

A preliminary framework to model wing polyphenism in aphids threatened by predators

inferred← citeshttps://doi.org/10.1002/arch.21614openalex-snapshot

Inhibition of histone acetylation and deacetylation enzymes affects longevity, development, and fecundity in the pea aphid (Acyrthosiphon pisum)

inferred← citeshttps://doi.org/10.1007/978-3-032-30270-0_7openalex-snapshot

Small Noncoding RNAs: Small Interfering RNAs and Piwi-interacting RNAs

inferred← citeshttps://doi.org/10.1007/978-94-007-7347-9_5openalex-snapshot

Integrating Phenotypic Plasticity Within an Ecological Genomics Framework: Recent Insights from the Genomics, Evolution, Ecology, and Fitness of Plasticity

inferred← citeshttps://doi.org/10.1007/s10340-017-0831-6openalex-snapshot

Effects of a genetically modified potato on a non-target aphid are outweighed by cultivar differences

inferred← citeshttps://doi.org/10.1007/s10340-017-0941-1openalex-snapshot

Unintended effects of a Phytophtora-resistant cisgenic potato clone on the potato aphid Macrosiphum euphorbiae and its parasitoid Aphidius ervi

inferred← citeshttps://doi.org/10.1007/s10886-018-0955-zopenalex-snapshot

Chemical Ecology and Sociality in Aphids: Opportunities and Directions

inferred← citeshttps://doi.org/10.1007/s12038-015-9506-8openalex-snapshot

Stochastic developmental variation, an epigenetic source of phenotypic diversity with far-reaching biological consequences

inferred← citeshttps://doi.org/10.1007/s12038-021-00138-6openalex-snapshot

Epigenetic variation in animal populations: Sources, extent, phenotypic implications, and ecological and evolutionary relevance

inferred← citeshttps://doi.org/10.1007/s13744-020-00777-8openalex-snapshot

Epigenetic Molecular Mechanisms in Insects

inferred← citeshttps://doi.org/10.1007/s40656-014-0004-3openalex-snapshot

Model organisms in evo-devo: promises and pitfalls of the comparative approach

inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00135-9openalex-snapshot

Developmental Plasticity and Phenotypic Evolution

inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.90723-4openalex-snapshot

Animal Personality

inferred← citeshttps://doi.org/10.1016/b978-0-443-15750-9.00113-0openalex-snapshot

Developmental Plasticity and Phenotypic Evolution

inferred← citeshttps://doi.org/10.1016/b978-0-443-18722-3.00022-0openalex-snapshot

Animal models in epigenetic research

inferred← citeshttps://doi.org/10.1016/b978-0-443-19051-3.00009-7openalex-snapshot

Role of epigenetic molecular mechanisms in insect evolutionary innovations

inferred← citeshttps://doi.org/10.1016/bs.aiip.2014.12.005openalex-snapshot

The Physiology and Genomics of Social Transitions in Aphids

inferred← citeshttps://doi.org/10.1016/bs.aiip.2017.03.001openalex-snapshot

Epigenetic Regulation of Longevity in Insects

inferred← citeshttps://doi.org/10.1016/bs.aiip.2019.01.005openalex-snapshot

Mechanisms regulating phenotypic plasticity in wing polyphenic insects

inferred← citeshttps://doi.org/10.1016/j.cbd.2020.100740openalex-snapshot

Transcriptomic changes in the pea aphid, Acyrthosiphon pisum: Effects of the seasonal timer and photoperiod

inferred← citeshttps://doi.org/10.1016/j.cois.2017.12.009openalex-snapshot

Rapid evolution of aphid pests in agricultural environments

inferred← citeshttps://doi.org/10.1016/j.cois.2020.09.016openalex-snapshot

Atypical insects: molecular mechanisms of unusual life history strategies

inferred← citeshttps://doi.org/10.1016/j.cois.2021.01.003openalex-snapshot

Aphid resistance is the future for soybean production, and has been since 2004: efforts towards a wider use of host plant resistance in soybean

inferred← citeshttps://doi.org/10.1016/j.cois.2021.10.004openalex-snapshot

The emerging role of epigenetic mechanisms in insect defense against pathogens.

inferred← citeshttps://doi.org/10.1016/j.ibmb.2020.103363openalex-snapshot

Soybean aphids adapted to host-plant resistance by down regulating putative effectors and up regulating transposable elements

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2015.02.009openalex-snapshot

Insects as models to study the epigenetic basis of disease

inferred← citeshttps://doi.org/10.1016/s2095-3119(19)62842-xopenalex-snapshot

Aphids and their transmitted potato viruses: A continuous challenges in potato crops

inferred← citeshttps://doi.org/10.1038/s41437-018-0108-8openalex-snapshot

Evolution without standing genetic variation: change in transgenerational plastic response under persistent predation pressure

inferred← citeshttps://doi.org/10.1038/s41598-019-45220-0openalex-snapshot

Different phenotypic plastic responses to predators observed among aphid lineages specialized on different host plants

inferred← citeshttps://doi.org/10.1080/24750263.2020.1779827openalex-snapshot

Micromorphology of the model species pea aphidAcyrthosiphon pisum(Hemiptera, Aphididae) with special emphasis on the sensilla structure

inferred← citeshttps://doi.org/10.1093/biolinnean/blz194openalex-snapshot

Aphids in focus: unravelling their complex ecology and evolution using genetic and molecular approaches

inferred← citeshttps://doi.org/10.1093/ee/nvv044openalex-snapshot

Do Bacterial Symbionts Govern Aphid's Dropping Behavior?

inferred← citeshttps://doi.org/10.1093/g3journal/jkab115openalex-snapshot

The boom and bust of the aphid’s essential amino acid metabolism across nymphal development

inferred← citeshttps://doi.org/10.1093/g3journal/jkaf013openalex-snapshot

Draft genome sequence of the glasshouse-potato aphid Aulacorthum solani

inferred← citeshttps://doi.org/10.1093/icb/icaa047openalex-snapshot

The Role of Stochasticity in the Origin of Epigenetic Variation in Animal Populations

inferred← citeshttps://doi.org/10.1093/jee/toy039openalex-snapshot

New Insights into the Methylation Status of Virulent Diuraphis noxia (Hemiptera: Aphididae) Biotypes

inferred← citeshttps://doi.org/10.1093/jisesa/ieab077openalex-snapshot

Multi-generational Effects of Different Resistant Wheat Varieties on Fitness of Sitobion avenae (Hemiptera: Aphididae)

inferred← citeshttps://doi.org/10.1093/jisesa/ieaf055openalex-snapshot

Investigating a role for piRNA-associated piwi genes in overcoming host-plant resistance in the soybean aphid, Aphis glycines

inferred← citeshttps://doi.org/10.1101/2023.02.15.528785openalex-snapshot

Striking clone-specific nymph deformity in pea aphid exposed to heat stress

inferred← citeshttps://doi.org/10.1101/2025.01.21.634144openalex-snapshot

Genomic connectivity and adaptation signals of the freshwater sponge Ephydatia muelleri across its distribution

inferred← citeshttps://doi.org/10.1111/1744-7917.12086openalex-snapshot

Reliable protocols for whole‐mount fluorescentin situhybridization (FISH) in the pea aphidAcyrthosiphon pisum: A comprehensive survey and analysis

inferred← citeshttps://doi.org/10.1111/1744-7917.12130openalex-snapshot

Aphids as models for ecological and evolutionary studies

inferred← citeshttps://doi.org/10.1111/bij.12816openalex-snapshot

The ‘generalism’ debate: misinterpreting the term in the empirical literature focusing on dietary breadth in insects

inferred← citeshttps://doi.org/10.1111/brv.12096openalex-snapshot

The cytogenetic architecture of the aphid genome

inferred← citeshttps://doi.org/10.1111/brv.12361openalex-snapshot

Aphid specialism as an example of ecological–evolutionary divergence

inferred← citeshttps://doi.org/10.1111/brv.12732openalex-snapshot

Eco‐evolutionary consequences of habitat warming and fragmentation in communities

inferred← citeshttps://doi.org/10.1111/eea.12431openalex-snapshot

Parasitoid‐induced transgenerational fecundity compensation in an aphid

inferred← citeshttps://doi.org/10.1111/ens.12174openalex-snapshot

Social aphids use their antennae to perceive density cue for soldier production

inferred← citeshttps://doi.org/10.1111/eva.12882openalex-snapshot

Population‐level inferences from environmental DNA—Current status and future perspectives

inferred← citeshttps://doi.org/10.1111/evo.12320openalex-snapshot

EPIGENETIC VARIATION IN ASEXUALLY REPRODUCING ORGANISMS

inferred← citeshttps://doi.org/10.1111/jbi.70142openalex-snapshot

Genomic Connectivity and Adaptation Signals of the Freshwater Sponge Ephydatia muelleri Across Its Distribution

inferred← citeshttps://doi.org/10.1111/mec.15216openalex-snapshot

Sex‐specific changes in the aphid DNA methylation landscape

inferred← citeshttps://doi.org/10.1111/mec.70536openalex-snapshot

Adaptation to Plant Defence in an Agricultural Insect Pest: Integrating Genome Scans and Gene Expression in the Soybean Aphid Reveals Multi‐Genic Pathways

inferred← citeshttps://doi.org/10.1111/mec.70553openalex-snapshot

Polyphenism Through RNA Chemical Modifications

inferred← citeshttps://doi.org/10.1111/phen.12021openalex-snapshot

Genome expression control during the photoperiodic response of aphids

inferred← citeshttps://doi.org/10.1127/entomologia/2025/3028openalex-snapshot

Insights into the triggering factors and determination mechanisms of host alternation in aphids

inferred← citeshttps://doi.org/10.1186/s12864-015-1525-1openalex-snapshot

The genome of Diuraphis noxia, a global aphid pest of small grains

inferred← citeshttps://doi.org/10.1201/b17450-10openalex-snapshot

Aphids (Hemiptera)

inferred← citeshttps://doi.org/10.1242/dev.204693openalex-snapshot

Polyphenisms: a developmental perspective

inferred← citeshttps://doi.org/10.1371/journal.pgen.1003872openalex-snapshot

Function and Evolution of DNA Methylation in Nasonia vitripennis

inferred← citeshttps://doi.org/10.1371/journal.pone.0071620openalex-snapshot

Genomic and Proteomic Analysis of Schizaphis graminum Reveals Cyclophilin Proteins Are Involved in the Transmission of Cereal Yellow Dwarf Virus

inferred← citeshttps://doi.org/10.1371/journal.pone.0282449openalex-snapshot

Exposure to heat stress leads to striking clone-specific nymph deformity in pea aphid

inferred← citeshttps://doi.org/10.18174/411738openalex-snapshot

Potatoes, pathogens and pests : effects of genetic modifi cation for plant resistance on non-target arthropods

inferred← citeshttps://doi.org/10.3389/finsc.2026.1883891openalex-snapshot

Banana aphid, Pentalonia nigronervosa (Hemiptera: Aphididae): ecology and implications for the integrated management of banana bunchy top disease

inferred← citeshttps://doi.org/10.3389/fnbeh.2014.00371openalex-snapshot

Dopaminergic modulation of phase reversal in desert locusts

inferred← citeshttps://doi.org/10.3389/fphys.2014.00001openalex-snapshot

Aphid polyphenisms: trans-generational developmental regulation through viviparity

inferred← citeshttps://doi.org/10.3390/biology13030160openalex-snapshot

The Fall Armyworm and Larger Grain Borer Pest Invasions in Africa: Drivers, Impacts and Implications for Food Systems

inferred← citeshttps://doi.org/10.3390/f10090720openalex-snapshot

Ophelimus migdanorum Molina-Mercader sp. nov. (Hymenoptera: Eulophidae): Application of Integrative Taxonomy for Disentangling a Polyphenism Case in Eucalyptus globulus Labill Forest in Chile

inferred← citeshttps://doi.org/10.3390/ijms18020357openalex-snapshot

Silencing of Two Insulin Receptor Genes Disrupts Nymph-Adult Transition of Alate Brown Citrus Aphid

inferred← citeshttps://doi.org/10.3390/insects10090260openalex-snapshot

The Effects of Different Diets and Transgenerational Stress on Acyrthosiphon pisum Development

inferred← citeshttps://doi.org/10.3390/insects11050265openalex-snapshot

Lysine Acetyltransferase p300/CBP Plays an Important Role in Reproduction, Embryogenesis and Longevity of the Pea Aphid Acyrthosiphon pisum

inferred← citeshttps://doi.org/10.3390/insects12060533openalex-snapshot

Male-Biased microRNA Discovery in the Pea Aphid

inferred← citeshttps://doi.org/10.3390/insects14020187openalex-snapshot

What Are the Functional Roles of Piwi Proteins and piRNAs in Insects?

inferred← citeshttps://doi.org/10.3390/insects9040153openalex-snapshot

Aspects, Including Pitfalls, of Temporal Sampling of Flying Insects, with Special Reference to Aphids

inferred← citeshttps://doi.org/10.3390/plants11081094openalex-snapshot

Screening and Evaluation for Antixenosis Resistance in Wheat Accessions and Varieties to Grain Aphid, Sitobion miscanthi (Takahashi) (Hemiptera: Aphididae)

inferred← citeshttps://doi.org/10.3791/58044openalex-snapshot

Maintaining Biological Cultures and Measuring Gene Expression in Aphis nerii: A Non-model System for Plant-insect Interactions

inferred← citeshttps://doi.org/10.3934/biophy.2015.4.412openalex-snapshot

Cytosine methylation in insects: new routes for the comprehension of insect complexity

inferred← citeshttps://doi.org/10.70675/1f4ffbd9z5ba2z45fbz8ef0z1cf7f769dd18openalex-snapshot

Modélisation d'un réseau de régulation d'ARN pour prédire des fonctions de gènes impliqués dans le mode de reproduction du puceron du pois

inferred← citeshttps://doi.org/10.70675/9ae42da2z5917z4b4ez9492z2ff2cb6ccba8openalex-snapshot

Genomic and ecological bases of aphids adaptation in the context of fruit tree domestication

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.